A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638011



Internal ID21586316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9295452..9295452hg38UCSC Ensembl
chr10:9337415..9337415hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071551
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638011
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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